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Suppression of inducible nitric oxide synthase expression induced by Toll-like receptor agonists by (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine

Authors
Eom, Sang-HoonGu, Gyo-JeongSuh, Chang WonKoh, Kwang OhKim, Dae YoungEom, Yong-BinYoun, Hyung-Sun
Issue Date
Oct-2013
Publisher
Elsevier BV
Keywords
Toll-like receptor; Inflammation; Nuclear factor-kappa B; Inducible nitric oxide synthase; (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine
Citation
International Immunopharmacology, v.17, no.2, pp 205 - 209
Pages
5
Journal Title
International Immunopharmacology
Volume
17
Number
2
Start Page
205
End Page
209
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/13331
DOI
10.1016/j.intimp.2013.06.006
ISSN
1567-5769
1878-1705
Abstract
Toll-like receptors (TLRs) recognize many pathogen-associated molecular patterns and induce innate immunity. TLR signaling pathways induce the activation of various transcription factors, such as nuclear factor-kappa B (NF-kappa B), leading to the induction of pro-inflammatory gene products, such as inducible nitric oxide synthase (iNOS). Here, we investigated the effect of an (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine (NVPP), previously synthesized in our laboratory, on inflammation by modulating NF-kappa B activation and iNOS expression induced by TLR agonists in murine macrophages. NVPP suppressed NF-kappa B activation and iNOS expression induced by lipopolysaccharide (TLR4 agonist), polyriboinosinic polyribocytidylic acid (TLR3 agonist), and macrophage-activating lipopeptide 2 kDa (TLR2 and TLR6 agonist). All the results suggest that NVPP is suitable for development as a new anti-inflammatory drug. (C) 2013 Elsevier B.V. All rights reserved.
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